- Salaire 32.74 à 41.97 $ selon l'expérience
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Temps plein
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Publié il y a 4 jour(s)
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1 poste à combler dès que possible
Description
- Identification and recruitment of study subjects including informed consent, randomization and implementation of study protocol (including follow-up visits with study participants)
- Maintain screening logs/records.
- Completion of Case Report Forms (CRFs).
- Serious adverse event management and reporting
- Manage all aspects of clinical trial start-up (contracts, ethics, in-hospital logistics, staff education)
- Bachelor's degree in a relevant field of study.
- Minimum 2 years previous experience in multi-center research studies/clinical trials.
- Experience with the management of large clinical research studies and or databases.
- Basic anatomy & physiology knowledge.
- Working knowledge of ICH-GCP Guidelines and international research requirements.
- Highly efficient computer skills, extensive experience with the Microsoft office suite.
Exigences
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